Details
Stereochemistry | ACHIRAL |
Molecular Formula | C6H10 |
Molecular Weight | 82.1436 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
C=CCCC=C
InChI
InChIKey=PYGSKMBEVAICCR-UHFFFAOYSA-N
InChI=1S/C6H10/c1-3-5-6-4-2/h3-4H,1-2,5-6H2
Molecular Formula | C6H10 |
Molecular Weight | 82.1436 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
The effect of rigidity, shape, unsaturation, and length on the anesthetic potency of hydrocarbons. | 2001 Jun |
|
Cyclocopolymerization: a mechanistic probe for dual-site alternating copolymerization of ethylene and alpha-olefins. | 2002 Apr 24 |
|
Conformation-dependent state selectivity in O-O cleavage of ONOONO: an "inorganic cope rearrangement" helps explain the observed negative activation energy in the oxidation of nitric oxide by dioxygen. | 2002 Aug 14 |
|
Convergent approach to pumiliotoxin alkaloids. Asymmetric total synthesis of (+)-pumiliotoxins A, B, and 225F. | 2002 Aug 9 |
|
Insertion/isomerization polymerization of 1,5-hexadiene: synthesis of functional propylene copolymers and block copolymers. | 2002 Oct 2 |
|
Double-chelation-assisted Rh-catalyzed intermolecular hydroacylation. | 2003 Apr 17 |
|
Dissociative and associative mechanisms of cope rearrangements of fluorinated 1,5-hexadienes and 2,2'-bis-methylenecyclopentanes. | 2003 Jun 4 |
|
Catalytic reduction of acetone by [(bpy)Rh]+: a theoretical mechanistic investigation and insight into cooperativity effects in this system. | 2003 Sep 17 |
|
Hydrosilylation of dienes by yttrium hydrido complexes containing a linked amido-cyclopentadienyl ligand. | 2004 Aug 7 |
|
New ligand systems incorporating two and three 4,4'-bipyridine units. Characterization of bi- and trimetallic rhodium and iridium complexes. | 2004 Nov 1 |
|
Influence of vinyl monomers and temperature on immobilization of cellulose 3,5-dimethylphenylcarbamate onto silica gel as chiral stationary phases for high-performance liquid chromatography. | 2006 Feb 3 |
|
One-pot synthesis of polysaccharide 3,5-dimethylphenylcarbamates having a random vinyl group for immobilization on silica gel as chiral stationary phases. | 2006 Jul |
|
Diastereomerically-specific zirconium complexes of chiral salan ligands: isospecific polymerization of 1-hexene and 4-methyl-1-pentene and cyclopolymerization of 1,5-hexadiene. | 2006 Oct 11 |
|
Allylic hydrogen abstraction II. H-abstraction from 1,4 type polyalkenes as a model for free radical trapping by polyunsaturated fatty acids (PUFAs). | 2007 Apr 28 |
|
Studies of the electron-promoted cope cyclization of 2,5-phenyl-substituted 1,5-hexadiene radical anions. | 2007 Jan 19 |
|
Calculational and experimental investigations of the pressure effects on radical-radical cross combination reactions: C2H5+C2H3. | 2007 Jul 26 |
|
Structure and reaction mechanism of basil eugenol synthase. | 2007 Oct 3 |
|
Structure-activity relationship (SAR) for the gas-phase ozonolysis of aliphatic alkenes and dialkenes. | 2008 Apr 7 |
|
QTAIM study on the degenerate cope rearrangements of 1,5-hexadiene and semibullvalene. | 2009 Apr 2 |
|
Cyclopolymerization of Nonconjugated Dienes with a Tridentate Phenoxyamine Hafnium Complex Supported by an sp(3) -C Donor: Isotactic Enchainment and Diastereoselective cis-Ring Closure. | 2009 Nov 19 |
|
Metalla-cope rearrangements: bridging organic and inorganic chemistry. | 2010 Aug 26 |
|
Insight into the phase equilibrium phenomena of systems containing dienes and dicyanamide ionic liquids as a new potential application. | 2010 Dec 2 |
|
On the relationship between structure and reaction rate in olefin ring-closing metathesis. | 2010 Oct 14 |
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 17:52:19 GMT 2023
by
admin
on
Fri Dec 15 17:52:19 GMT 2023
|
Record UNII |
4MTZ4764FI
|
Record Status |
Validated (UNII)
|
Record Version |
|
-
Download
Name | Type | Language | ||
---|---|---|---|---|
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Common Name | English |
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
11598
Created by
admin on Fri Dec 15 17:52:19 GMT 2023 , Edited by admin on Fri Dec 15 17:52:19 GMT 2023
|
PRIMARY | |||
|
592-42-7
Created by
admin on Fri Dec 15 17:52:19 GMT 2023 , Edited by admin on Fri Dec 15 17:52:19 GMT 2023
|
PRIMARY | |||
|
60690
Created by
admin on Fri Dec 15 17:52:19 GMT 2023 , Edited by admin on Fri Dec 15 17:52:19 GMT 2023
|
PRIMARY | |||
|
4MTZ4764FI
Created by
admin on Fri Dec 15 17:52:19 GMT 2023 , Edited by admin on Fri Dec 15 17:52:19 GMT 2023
|
PRIMARY | |||
|
C545783
Created by
admin on Fri Dec 15 17:52:19 GMT 2023 , Edited by admin on Fri Dec 15 17:52:19 GMT 2023
|
PRIMARY | |||
|
209-754-7
Created by
admin on Fri Dec 15 17:52:19 GMT 2023 , Edited by admin on Fri Dec 15 17:52:19 GMT 2023
|
PRIMARY | |||
|
1,5-Hexadiene
Created by
admin on Fri Dec 15 17:52:19 GMT 2023 , Edited by admin on Fri Dec 15 17:52:19 GMT 2023
|
PRIMARY | |||
|
DTXSID4049323
Created by
admin on Fri Dec 15 17:52:19 GMT 2023 , Edited by admin on Fri Dec 15 17:52:19 GMT 2023
|
PRIMARY |